反应 #60715

ord-43c9b695c3ea4d05bc25b760ca2ee2a1

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他afforded
  2. 2
    其他after purification (SiO2: 8:2:1 hexane:EtOAc:isopropylamine), 115 mg (30%) of the title compound

实验过程

Using alkylation method B, 3-chloro-N-[1-(4-fluoro-phenyl)-2-(piperidin-4-ylmethoxy)ethyl]-1H-indole-6-carboxamide (373 mg, 0.87 mmol) and paraformaldehyde (520 mg, 17 mmol) afforded, after purification (SiO2: 8:2:1 hexane:EtOAc:isopropylamine), 115 mg (30%) of the title compound.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07427632B2uspto-grants-2008_09